FOXA1 in HPV associated carcinomas: Its expression in carcinomas of the head and neck and of the uterine cervix

13Citations
Citations of this article
24Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Background FOXA1 is a major transcription factor involved in the action of human papilloma virus (HPV). However, it has been never studied in HPV-associated tumors. Aim of the study To investigate its expression in cervical and head and neck tumors. Material and methods 63 cervical carcinomas/dysplasias and 152 head and neck squamous cell carcinomas (HNSCC) were immunohistochemically studied for the expression of FOXA1. Results 63.1% of cervical SCC and 40.7% of endocervical adenocarcinomas strongly expressed FOXA1. Most (90%) pre-invasive lesions (CIN3 and in situ adenocarcinomas) strongly expressed FOXA1 and this difference from invasive lesions was statistically significant (p = 0.005). No association with clinicopathological factors was found. 51.3% of HNSCC expressed FOXA1. In these tumors, FOXA1 expression was associated with the non-keratinizing morphology but not with the HPV/p16 status neither other clinicopathological features. Of normal structures, salivary glands, endocervical glands and basal/parabasal cell layer of squamous epithelium of both uterine cervix and head and neck mucosa, all strongly expressed FOXA1. Conclusion FOXA1 is expressed by basal cells of squamous epithelium, pre-invasion lesions of the uterine cervix and the head/neck and almost half invasive cervical and head/neck carcinomas, supporting its possible implication in HPV pathogenesis.

Cite

CITATION STYLE

APA

Karpathiou, G., Da Cruz, V., Casteillo, F., Mobarki, M., Dumollard, J. M., Chauleur, C., … Peoc’h, M. (2017). FOXA1 in HPV associated carcinomas: Its expression in carcinomas of the head and neck and of the uterine cervix. Experimental and Molecular Pathology, 102(2), 230–236. https://doi.org/10.1016/j.yexmp.2017.02.010

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free